Fpg-和MutY联合缺乏对M13mp10 lacZα基因自发和γ辐射诱导突变谱的影响

Gitta K Kuipers, Ben J Slotman, Hester A Poldervaart, Carola A Reitsma-Wijker, M.Vincent M Lafleur
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引用次数: 12

摘要

7,8-二氢-8-氧鸟嘌呤(8oxoG)是自发形成和γ辐射后最主要的DNA氧化损伤之一。这种8oxoG是一种致突变性病变,因为它可以与腺嘌呤而不是正确的胞嘧啶错误配对,导致G:C到T:a的转换。在大肠杆菌中,碱基切除修复(BER)是修复8oxoG和其他氧化性DNA损伤的最重要的修复系统之一。大肠杆菌BER的一个重要部分是所谓的GO系统,该系统由三种修复酶MutM(Fpg)、MutY和MutT组成,它们都参与8oxoG或8oxoGmispairs的修复。本研究的目的是确定Fpg-和MutY联合缺乏对lacZα基因自发和γ辐射诱导突变谱的影响。为此,将插入lacZα基因作为突变靶序列的非辐照或γ辐照双链(ds)M13mp10 DNA转染到Fpg和MutY都缺乏的大肠杆菌菌株(BH1040)中。将得到的突变谱与早期研究中确定的fpg−大肠杆菌菌株(BH410)和野生型大肠杆菌株(JM105)的突变谱进行比较。本研究的结果表明,与Fpg−和野生型菌株相比,Fpg-和MutY联合缺乏导致BH1040(Fpg−MutY−)的自发和γ辐射诱导突变谱中G:C到T:a的颠换大幅增加。在BH1040(fpg−mutY−)的自发和γ辐射诱导的突变谱中,除了G:C到T:A的颠换水平增加外,G:C和移码突变也增加。
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The influence of combined Fpg- and MutY-deficiency on the spontaneous and γ-radiation-induced mutation spectrum in the lacZα gene of M13mp10

One of the most predominating oxidative DNA damages, both spontaneously formed and after γ-radiation is 7,8-dihydro-8-oxoguanine (8oxoG). This 8oxoG is a mutagenic lesion because it can mispair with adenine instead of the correct cytosine leading to G:C to T:A transversions. In Escherichia coli (E. Coli) base excision repair (BER) is one of the most important repair systems for the repair of 8oxoG and other oxidative DNA damage. An important part of BER in E. coli is the so-called GO system which consists of three repair enzymes, MutM (Fpg), MutY and MutT which are all involved in repair of 8oxoG or 8oxoG mispairs. The aim of this study is to determine the effect of combined Fpg- and MutY-deficiency on the spontaneous and γ-radiation-induced mutation spectrum of the lacZα gene. For that purpose, non-irradiated or γ-irradiated double-stranded (ds) M13mp10 DNA, with the lacZα gene inserted as mutational target sequence was transfected into an E. coli strain which is deficient in both Fpg and MutY (BH1040). The resulting mutation spectra were compared with the mutation spectra of a fpg E. coli strain (BH410) and a wild type E. coli strain (JM105) which were determined in an earlier study. The results of the present study indicate that combined Fpg- and MutY-deficiency induces a large increase in G:C to T:A transversions in both the spontaneous and γ-radiation-induced mutation spectra of BH1040 (fpgmutY) as compared to the fpg and the wild type strain. Besides the increased levels of G:C to T:A transversions, there is also an increase in G:C to C:G transversions and frameshift mutations in both the spontaneous and γ-radiation-induced mutation spectra of BH1040 (fpgmutY).

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S. cerevisiae has three pathways for DNA interstrand crosslink repair Molecular characterization of ionizing radiation-hypersensitive mutant M10 cells Backbone dynamics of DNA containing 8-oxoguanine: importance for substrate recognition by base excision repair glycosylases Relationship between base excision repair capacity and DNA alkylating agent sensitivity in mouse monocytes Disruption of Xpg increases spontaneous mutation frequency, particularly A:T to C:G transversion
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